Preferred Name |
systemic scleroderma |
|
Synonyms |
Scleroderma |
|
Definitions |
A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. |
|
ID |
http://purl.obolibrary.org/obo/DOID_418 |
|
database_cross_reference |
MESH:D012595 UMLS_CUI:C0036421 OMIM:181750 SNOMEDCT_US_2020_03_01:89155008 ICD10CM:M34.0 EFO:0000717 ICD9CM:710.1 GARD:9748 NCI:C72070 |
|
has exact synonym |
Scleroderma progressive systemic sclerosis Scleroderma syndrome systemic sclerosis |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:418 |
|
imported from | ||
in_subset | ||
label |
systemic scleroderma |
|
notation |
DOID:418 |
|
prefLabel |
systemic scleroderma |
|
textual definition |
A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. |
|
subClassOf |
The BioAssay Ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.
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Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.
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References (optional)
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